SLC10A2, solute carrier family 10 member 2, 6555

N. diseases: 66; N. variants: 9
Disease: Cholelithiasis ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs56398830
rs56398830 		0.925 0.040 13 103049340 missense variant G/A;T snv 1.0E-02
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis 		Digestive System Diseases 0.020 1.000 2 2018 2019
dbSNP: rs9514089
rs9514089 		0.882 0.080 13 103058487 intron variant T/C snv 0.41
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis 		Digestive System Diseases 0.020 0.500 2 2009 2011
dbSNP: rs55971546
rs55971546 		1.000 0.040 13 103065958 missense variant C/A;T snv 4.0E-06; 2.7E-02
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis 		Digestive System Diseases 0.010 1.000 1 2018 2018